Dental agenesis is the most common developmental anomaly in humans and is frequently
associated with several other oral abnormalities. Whereas the incidence of missing teeth …

Teeth organogenesis develops through a well-ordered series of inductive events involving
genes and BMP, FGF, SHH and WNT represent the main signalling pathways that regulate …

Tooth agenesis or hypodontia, failure to develop all normally developing teeth, is one of the
most common developmental anomalies in man. Common forms, including third molar …

Tooth agenesis is one of the most common congenital malformations in humans.
Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be …

Paired box 9 (PAX9) is one of the best‐known transcription factors involved in the
development of human dentition. Mutations in PAX9 gene could, therefore, seriously …

The most common outcome of defective dental morphogenesis in human patients is dental
agenesis (absence of teeth). This may affect either the primary or permanent dentition and …

Zusammenfassung Fragestellung Identifizierung aller bekannten Genmutationen, die mit der
Entstehung nonsyndromaler Oligodontien assoziiert werden. Methodik. Eine systematische …

Objectives: To evaluate the prevalence of dental agenesis and its possible association with
other developmental dental anomalies and systemic entities. Setting and Sample …

AIM: An association between tooth agenesis and taurodontism has been suggested. To
verify if tooth agenesis and taurodontism are associated within families and specific patterns …

Background: Non-syndromic oligodontia is characterized by the absence of six or more
permanent teeth, excluding third molars, and can have aesthetic, masticatory, and …